Job Description:
• Work closely with study leads to design client-facing real-world oncology studies with high quality study protocols and statistical analysis plans
• Collaborate with statistical programmers to ensure accurate implementation of analyses in accordance with study specifications
• Assist in interpretation and presentation of study findings through study reports and presentations to clients
• Contribute to discussions with cross-functional stakeholders, including oncologists and project managers, to execute and deliver on projects in an accurate, effective, and timely manner
• Continue to develop your understanding of epidemiological and statistical approaches for analyzing observational real-world data and deepen your understanding of cancer biology, therapies, and outcomes across multiple major tumor types
Requirements:
• You hold a Master’s degree in Epidemiology, Biostatistics, Health Economics and Outcomes Research, Health Policy (or closely related field) with 2 - 3 years of relevant experience or a Bachelor’s degree in one of those fields with 4-5 years
• You have experience working in a pharmaceutical/HEOR consulting environment
• You have experience with observational datasets (e.g., registries, healthcare claims, or electronic health records)
• You have strong communication skills, with experience contributing to study documentation
• You have effective organizational, time-management, and prioritization and skills necessary to contribute to multiple high-visibility projects in a timely fashion
• You have an agile mindset and adapt quickly to changes in project direction
• You are able to quickly learn and apply new information, skills and procedures
• You are passionate about our mission to improve healthcare through technology
• You have oncology experience
Benefits:
• Flexible work arrangements
• Professional development opportunities
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